CA2042857C - Curable bismaleide systems - Google Patents
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/12—Unsaturated polyimide precursors
- C08G73/126—Unsaturated polyimide precursors the unsaturated precursors being wholly aromatic
- C08G73/127—Unsaturated polyimide precursors the unsaturated precursors being wholly aromatic containing oxygen in the form of ether bonds in the main chain
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/36—Amides or imides
- C08F222/40—Imides, e.g. cyclic imides
- C08F222/404—Imides, e.g. cyclic imides substituted imides comprising oxygen other than the carboxy oxygen
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/12—Unsaturated polyimide precursors
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/12—Unsaturated polyimide precursors
- C08G73/124—Unsaturated polyimide precursors the unsaturated precursors containing oxygen in the form of ether bonds in the main chain
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/12—Unsaturated polyimide precursors
- C08G73/125—Unsaturated polyimide precursors the unsaturated precursors containing atoms other than carbon, hydrogen, oxygen or nitrogen in the main chain
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/12—Unsaturated polyimide precursors
- C08G73/126—Unsaturated polyimide precursors the unsaturated precursors being wholly aromatic
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
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- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
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- Macromonomer-Based Addition Polymer (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Polyethers (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
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Abstract
There are disclosed novel compositions comprising a) at least one bismaleide, b) at least one mono- or polynuclear alkenylphenol, one alkenylphenol ether or a mixture thereof, wherein the alkenyl group contains at least three 3 carbon atoms, c) a copolyether resin.
The compositions of the invention can be cured to products having improved toughness and high glass transition temperatures. These products are suitable for making high-performance moulded articles which can be subjected to high temperatures, for example fibre-reinforced composites, structural adhesives, laminating or electrical insulating resins.
The compositions of the invention can be cured to products having improved toughness and high glass transition temperatures. These products are suitable for making high-performance moulded articles which can be subjected to high temperatures, for example fibre-reinforced composites, structural adhesives, laminating or electrical insulating resins.
Description
Novel curable bismaleide systems The present invention relates to compositions comprising bismaleides, an alkenylphenol and/or an alkenylphenol ether and a copolyether resin, as well as a process for making cured products using the compositions of the invention.
A process for the preparation of crosslinked polymers containing imide groups by reacting polymaleimides and alkenylphenols and/or alkenylphenol ethers is disclosed in US patent specification 4 100140. Curable compositions of propenyl-substituted copolyether resins and bismaleimides (BMI) are disclosed in EP-A 327 498, which compositions may be used and processed in the conventional manner for thermoplastics and exhibit the characteristic properties of thern~oset plastics after curing, for example high strength and glass transition temperature.
It is the object of this invention to provide BMI systems which have greater toughness and high glass transition temperatures and which can be processed and cured at relatively low temperatures.
Specifically, the invention relates to compositions comprising a) at least one bismaleimide of formula I
O O
t R2 ~O O _R2 wherein Rt and R2 are each independently of the other hydrogen or methyl and A
is a divalent organic radical of 2 to 30 carbon atoms, b) at least one mononuclear or polynuclear alkenylphenol, an alkenylphenol ether or a mixture thereof, wherein the alkenyl group contains at least three carbon atoms, c) a copolyether resin containing end groups -OR3 attached direct to phenyl nuclei and 1 to 50 mol % of structural repeating units of formula II
(R5)m (RS) m (Rs) / / /
O X O Y
w w ~ (B), (Ra) P (Ra) P
and 50 to 99 mol % of structural repeating units of formula III
(R~) t / i O - E - O ~ Z (III), (R~) t wherein R3 is hydrogen or a radical of formulae IV to VII
/ /
(Ra) q (N), N(R9R~o~ 4 \ \
O
O
N G q (VI], - CH2~ (VII), R»
O
-CH (C6H5) -, X is a direct bond or a group of formulae -CrHzr-, -C (CF3) 2-, -S-, -SO-, -SO2-, -O- or -CO-, r is 1 to 20, R4 is prop-1-enyl or 2-methylprop-1-enyl, R5, R6 and R7 are each independently of one another C1-C4alkyl, C1-C4alkoxy or chloro or bromo, m, n and t are each independently of one another 0, 1 or 2a 2, p is 1 or 2, E is a divalent radical of a bisphenol after removal of both phenolic hydroxyl groups, which radical is unsubstituted or substituted by one or two C1-C4alkyl or C1-C4alkoxy groups or one or two chlorine or bromine atoms, Y
and Z are each independently of the other -CO- or -SOz-, R$ is vinyl, ethynyl, allyl, methallyl, prop-1-enyl or 2-methylprop-1-enyl, R9 and Rlo are each independently of the other hydrogen, allyl or methallyl, R11 is hydrogen or methyl, q is 1 or 2, G is a group of formulae VIII or IX, ~~~8~~
A process for the preparation of crosslinked polymers containing imide groups by reacting polymaleimides and alkenylphenols and/or alkenylphenol ethers is disclosed in US patent specification 4 100140. Curable compositions of propenyl-substituted copolyether resins and bismaleimides (BMI) are disclosed in EP-A 327 498, which compositions may be used and processed in the conventional manner for thermoplastics and exhibit the characteristic properties of thern~oset plastics after curing, for example high strength and glass transition temperature.
It is the object of this invention to provide BMI systems which have greater toughness and high glass transition temperatures and which can be processed and cured at relatively low temperatures.
Specifically, the invention relates to compositions comprising a) at least one bismaleimide of formula I
O O
t R2 ~O O _R2 wherein Rt and R2 are each independently of the other hydrogen or methyl and A
is a divalent organic radical of 2 to 30 carbon atoms, b) at least one mononuclear or polynuclear alkenylphenol, an alkenylphenol ether or a mixture thereof, wherein the alkenyl group contains at least three carbon atoms, c) a copolyether resin containing end groups -OR3 attached direct to phenyl nuclei and 1 to 50 mol % of structural repeating units of formula II
(R5)m (RS) m (Rs) / / /
O X O Y
w w ~ (B), (Ra) P (Ra) P
and 50 to 99 mol % of structural repeating units of formula III
(R~) t / i O - E - O ~ Z (III), (R~) t wherein R3 is hydrogen or a radical of formulae IV to VII
/ /
(Ra) q (N), N(R9R~o~ 4 \ \
O
O
N G q (VI], - CH2~ (VII), R»
O
-CH (C6H5) -, X is a direct bond or a group of formulae -CrHzr-, -C (CF3) 2-, -S-, -SO-, -SO2-, -O- or -CO-, r is 1 to 20, R4 is prop-1-enyl or 2-methylprop-1-enyl, R5, R6 and R7 are each independently of one another C1-C4alkyl, C1-C4alkoxy or chloro or bromo, m, n and t are each independently of one another 0, 1 or 2a 2, p is 1 or 2, E is a divalent radical of a bisphenol after removal of both phenolic hydroxyl groups, which radical is unsubstituted or substituted by one or two C1-C4alkyl or C1-C4alkoxy groups or one or two chlorine or bromine atoms, Y
and Z are each independently of the other -CO- or -SOz-, R$ is vinyl, ethynyl, allyl, methallyl, prop-1-enyl or 2-methylprop-1-enyl, R9 and Rlo are each independently of the other hydrogen, allyl or methallyl, R11 is hydrogen or methyl, q is 1 or 2, G is a group of formulae VIII or IX, ~~~8~~
(R4~ s - CH- CH- (VIII), (IX), Rtz wherein R12 is hydrogen or methyl and s is 0, 1 or 2.
The bismaleimides of formula I are known compounds and are described, for example, in US
patent specification ~ 100 140. They are preferably compounds of formula I, whezein Rl and RZ are hydrogen.
Preferzed bismaleides are compounds of formula I, wherein A is -C2H2"-, in which a is 2-20, phenylene, xylylene, naphthylene, cyclopentylene, 1,5,5-trimethylcyclohexyl-1,3-ene; cyclo-hexyl-1,4-ene; 1,4-bis(methylene)cyclohexylene, the radical of 4,4'-bis(eyclohexyl)methane or a group of formula X, Rta Rts Rts Rta T ~ ~ (x)~
Rts Rts Rts ~Rt3 wherein R13 and R14 are identical or different and are each hydrogen or Cl-C4alkyl, Rls and Rlb are each independently of the other a hydrogen ar halogen atom, and T
is a direct bond, methylene, 2,2-propylidene, -S-, -SO-, -SOZ-, -O- or -CO-.
Particularly preferred compounds of formula I are those wherein A is a group of formula X, wherein R13 and Rl~ are each independently of the other hydrogen, methyl or ethyl, Rls and R16 are hydrogen and T is methylene.
Methylenebis(phenylmaleimide) is most especially preferred.
Ivlixtures of two or more different bismaleimides may of course also be used.
Representative examples of bismaleimides of formula I are: N,N'-ethylenebismaleimide, N,N'-hexamethylenebismaleimide, N,N'-trimethylhexylenebismaleimide, N,N'-m-pheny-~~~~~~~1 lenebismaleimide, N,N'-4,4'-diphenylmethanebismaleimide, N,N'-4,4'-Biphenyl ether bismaleimide, N,N'-(1,5,5-trimethylcyclohexyl-1,3-ene)bismaleimide, N,N-4,4'-dicyclo-hexylmethanebismaleimide, N,N'-p-xylylenebismaleimide, N,N'-4,4'-bis(2-ethyl-6-me-thylphenyl)methanebismaleimide, N,N'-4,4'-bis(2,6-dimethylphenyl)methanebismale-imide, N,N'-4,4'-bis(2,6-diethylphenyl)methanebismaleimide, N,N'-4,4'-bis(2,6-diiso-propylphenyl)methanebismaleimide, N,N'-4,4'-bis(2-ethyl-6-isopropylphenyl)me-thanebismaleimide, N,N'-4,4'-bis(3-chloro-2,6-diethylphenyl)methanebismaleimide.
The compounds of formula I are prepared by known methods, for example by xeacting the unsubstituted or substituted malefic anhydride with the corresponding diamines.
Conventional methods are described in US patent specification 3 010 290 or in GB patent specification 1 137 592.
Alkenylphenols or alkenylphenol ethers are known compounds and are described, for example, in US patent specification 4100140. Preferred compounds are those of formula XI
Rig Ris OR21(~).
Rye R2o wherein Q is a direct bond, -CH2-, -C(CH3)2-, -S-, -SO-, -S02-, -O- or -CO-, Rte, R18, R~9 and R2o are each independently of one another hydrogen or C3-CloaLtCenyl, and at least one of Rl~ to R2o is an alkenyl group, and RZt is hydrogen, Ci-Cloalkyl, C6-Cloaryl or C3-CtoaIkenyl.
The alkenyl group in compounds of formula XI is preferably an allyl, methallyl or propenyl group.
In the compositions of this invention it is preferred to use compounds of formula XI, wherein Q is -CI-I2-, -C(CH3)2-, -S-, -S02-, -O- or -CO-, Rl~ and Rl9 are each allyl, Rl8 and R2o are each hydrogen and R21 is hydrogen.
Particularly preferred alkenylphenols of formula XI are those wherein Q is -C(CH3)2-, R17 and Rt9 are each allyl, Rt8 and RZO are each hydrogen, and R2t is hydrogen.
It is preferred to use compounds of formula XI which contain two alkenyl groups in each molecule.
r~~~~~~~fi~
The bismaleimides of formula I are known compounds and are described, for example, in US
patent specification ~ 100 140. They are preferably compounds of formula I, whezein Rl and RZ are hydrogen.
Preferzed bismaleides are compounds of formula I, wherein A is -C2H2"-, in which a is 2-20, phenylene, xylylene, naphthylene, cyclopentylene, 1,5,5-trimethylcyclohexyl-1,3-ene; cyclo-hexyl-1,4-ene; 1,4-bis(methylene)cyclohexylene, the radical of 4,4'-bis(eyclohexyl)methane or a group of formula X, Rta Rts Rts Rta T ~ ~ (x)~
Rts Rts Rts ~Rt3 wherein R13 and R14 are identical or different and are each hydrogen or Cl-C4alkyl, Rls and Rlb are each independently of the other a hydrogen ar halogen atom, and T
is a direct bond, methylene, 2,2-propylidene, -S-, -SO-, -SOZ-, -O- or -CO-.
Particularly preferred compounds of formula I are those wherein A is a group of formula X, wherein R13 and Rl~ are each independently of the other hydrogen, methyl or ethyl, Rls and R16 are hydrogen and T is methylene.
Methylenebis(phenylmaleimide) is most especially preferred.
Ivlixtures of two or more different bismaleimides may of course also be used.
Representative examples of bismaleimides of formula I are: N,N'-ethylenebismaleimide, N,N'-hexamethylenebismaleimide, N,N'-trimethylhexylenebismaleimide, N,N'-m-pheny-~~~~~~~1 lenebismaleimide, N,N'-4,4'-diphenylmethanebismaleimide, N,N'-4,4'-Biphenyl ether bismaleimide, N,N'-(1,5,5-trimethylcyclohexyl-1,3-ene)bismaleimide, N,N-4,4'-dicyclo-hexylmethanebismaleimide, N,N'-p-xylylenebismaleimide, N,N'-4,4'-bis(2-ethyl-6-me-thylphenyl)methanebismaleimide, N,N'-4,4'-bis(2,6-dimethylphenyl)methanebismale-imide, N,N'-4,4'-bis(2,6-diethylphenyl)methanebismaleimide, N,N'-4,4'-bis(2,6-diiso-propylphenyl)methanebismaleimide, N,N'-4,4'-bis(2-ethyl-6-isopropylphenyl)me-thanebismaleimide, N,N'-4,4'-bis(3-chloro-2,6-diethylphenyl)methanebismaleimide.
The compounds of formula I are prepared by known methods, for example by xeacting the unsubstituted or substituted malefic anhydride with the corresponding diamines.
Conventional methods are described in US patent specification 3 010 290 or in GB patent specification 1 137 592.
Alkenylphenols or alkenylphenol ethers are known compounds and are described, for example, in US patent specification 4100140. Preferred compounds are those of formula XI
Rig Ris OR21(~).
Rye R2o wherein Q is a direct bond, -CH2-, -C(CH3)2-, -S-, -SO-, -S02-, -O- or -CO-, Rte, R18, R~9 and R2o are each independently of one another hydrogen or C3-CloaLtCenyl, and at least one of Rl~ to R2o is an alkenyl group, and RZt is hydrogen, Ci-Cloalkyl, C6-Cloaryl or C3-CtoaIkenyl.
The alkenyl group in compounds of formula XI is preferably an allyl, methallyl or propenyl group.
In the compositions of this invention it is preferred to use compounds of formula XI, wherein Q is -CI-I2-, -C(CH3)2-, -S-, -S02-, -O- or -CO-, Rl~ and Rl9 are each allyl, Rl8 and R2o are each hydrogen and R21 is hydrogen.
Particularly preferred alkenylphenols of formula XI are those wherein Q is -C(CH3)2-, R17 and Rt9 are each allyl, Rt8 and RZO are each hydrogen, and R2t is hydrogen.
It is preferred to use compounds of formula XI which contain two alkenyl groups in each molecule.
r~~~~~~~fi~
Typical examples of alkenylphenols or alkenylphenol ethers which may be used in the compositions of this invention are:
o,o'-diallyl bisphenol A, o,o'-diallyl bisphenol F, 4,4'-dihydroxy-3,3'-diallyldiphenyl, 4,4'-diallyloxydiphenyl.
The corresponding methallyl compounds can also be used.
Alkenylphenols are obtained by (thermal) Claisen rearrangement of the alkenyl ethers of phenols (q.v. USP 4 100 140). The alkenyl ethers are also obtained by known methods, for example by reacting phenols with allyl chloride in the presence of an alkali metal hydroxide.
It is also possible to use mixtures of compounds which contain only one hydroxyl group and only one alkenyl group in the aromatic nucleus with compounds which contain several hydroxyl groups and/or several alkenyl groups in the aromatic nucleus, or mixtures of the corresponding phenyl ethers of these compounds.
The alkenyl-substituted copolyether resins containing structural repeating units of formulae II and III are disclosed in EP-A 327 498.
In the compositions of the invention it is preferred to use polyether sulfones/ketones containing structural repeating units of formulae II and III, wherein the indices m, n and t are 0 and p an q are I.
R3 is preferably hydrogen or a radical of formula V, wherein Rg and Rlp are each hydrogen and q is 1.
The preferred meaning of X in formula II is a direct bond, -CH2-, -CH(CH3)-, -CH(C6H5)-, W(~3)2-~ -~(~3)2': S-, -SO-, -SOZ-, -O- or -CO-.
Most preferably X is a direct bond, -CH2- or -C(CH3)2-.
The preferred meaning of Rø is prop-1-enyl.
The substituents I~ in formula II are preferably each in ortho-position to the phenolic -O- atom.
o,o'-diallyl bisphenol A, o,o'-diallyl bisphenol F, 4,4'-dihydroxy-3,3'-diallyldiphenyl, 4,4'-diallyloxydiphenyl.
The corresponding methallyl compounds can also be used.
Alkenylphenols are obtained by (thermal) Claisen rearrangement of the alkenyl ethers of phenols (q.v. USP 4 100 140). The alkenyl ethers are also obtained by known methods, for example by reacting phenols with allyl chloride in the presence of an alkali metal hydroxide.
It is also possible to use mixtures of compounds which contain only one hydroxyl group and only one alkenyl group in the aromatic nucleus with compounds which contain several hydroxyl groups and/or several alkenyl groups in the aromatic nucleus, or mixtures of the corresponding phenyl ethers of these compounds.
The alkenyl-substituted copolyether resins containing structural repeating units of formulae II and III are disclosed in EP-A 327 498.
In the compositions of the invention it is preferred to use polyether sulfones/ketones containing structural repeating units of formulae II and III, wherein the indices m, n and t are 0 and p an q are I.
R3 is preferably hydrogen or a radical of formula V, wherein Rg and Rlp are each hydrogen and q is 1.
The preferred meaning of X in formula II is a direct bond, -CH2-, -CH(CH3)-, -CH(C6H5)-, W(~3)2-~ -~(~3)2': S-, -SO-, -SOZ-, -O- or -CO-.
Most preferably X is a direct bond, -CH2- or -C(CH3)2-.
The preferred meaning of Rø is prop-1-enyl.
The substituents I~ in formula II are preferably each in ortho-position to the phenolic -O- atom.
The group E as divalent radical of a bisphenol is normally the divalent radical of a mono- or polynuclear carbocylic-aromatic phenol, preferably the radical of a mono-or binuclear carbocylic-aromatic phenol, both aromatic nuclei of which are fused or linked to each other through a linking group.
Preferred radicals E have the formulae XII to XIV
/ / \
). I (xrm, /. ~ ~ /
\ \ /
to wherein L is a direct bond, a group of formulae -CrH2r- (r=1 to 20) , -CH (C6H5) -, -C (CF3) 2-, -S-, -SOZ-, -O- or -CO-, or is a group of formula XV or XVI
(XV), (XV~.
Most particularly preferred radicals E have the formulae XII, XIII or XIV, wherein L is a direct bond or a group of formula -CH2-, -CH (CH3) -, -CH (C2H5) -, -C (CH3) (CZHS) -, -C (CF3) 2-, -S-, -S02- or -CO- .
Y and Z preferably have the same meaning.
Especially preferred components c) are copolyether resins comprising 2 to 30 mol % of structural repeating units of formula II and 98 to 70 mol % of structural repeating units of formula III and having an average molecular weight (number average) of 2,000 to 30,000, preferably 5,000 to 20,000.
6a The compositions of this invention preferably contain 5-100 % by weight, most preferably 10-50 % by weight of component c), based on the amount of component a).
The molar ratio of component b):a) is preferably (0.5-1.4):1, preferably (0.7-1.2):1.
The compositions of the invention are cured in known manner, typically in the temperature range from 100 to 300°C for a time sufficient to effect the cure.
The expression "cure" as used herein means the conversion of low viscosity resin compositions into insoluble and infusible crosslinked products. It is thus possible to prepare high-performance _7_ moulded articles such as (fibre-reinforced} composites, structural adhesives, laminating or electrical insulating resins which can be subjected to high temperatures.
The compositions of the invention can be mixed at any stage prior to the cure with conventional modifiers such as extenders, fillers and reinforcing agents, pigments, dyes, organic solvents, plasticisers, tackifiers, tougheners, rubbers, accelerators, flame retardants or thixotropic agents.
Illustrative examples of suitable modifiers are: coal tar, bitumen, glass fibres, boron fibres, carbon fibres, cellulose, polyethylene powder, polypropylene powder, mica, asbestos, quartz powder, gypsum, antimony trioxide, bentones, silica aerogel ("aerosil"), lithopone, barites, titanium dioxide, carbon black, graphite, iron oxide, metal powders such as aluminium powder or iron powder, silicones, cellulose acetate butyrate, polyvinyl butyrate, waxes and stearates.
Suitable additional tougheners are products which are known to the skilled parson, such as polyimicles (for example Matrimid~ 5218, Ciba-Geigy), polyether imides (for example Ultem~
1000, General Electric), polyether sulfones or ketanes (for example VlCtrex~, ICI or Ultrason~ E, BASF) or polyhydantoins.
The compositions of the invention are very readily processible, have good solubility in customary organic solvents, good stability in the melt or in solution, and the cured products made from them have good thermal and mechanical properties. The products obtained have enhanced toughness and high glass transition temperatures.
The invention accordingly also relates to a process for the preparation of cured products, which comprises the use of the novel compositions.
The compositions of this invention can be used in different fields, for example in prepregs, laminates, composites, printed circuit boards, castings, mouldings, adhesives and coatings. A
particularly interesting utility is the fabrication of fibre-reinforced composites.
Example 1 In a round flask, 75 g of o,o'-diallyl bisphenel A is heated to 150°C
and, with stirring, 10 g of a copolyether resin prepared according to Example 1 of EP-A 327 498 are added.
When the resin has completely dissolved (15 min), 100 g of methylenebisphenylmaleimide are added, with stirring.
The mixture is then stirred for a further 15 minutes at 125-130°C, degassed under a water jet vacuum, and poured into an aluminium mould (4 mm) of 180°C. The mixture is fully cured for 1 h at 180°C, for 2 h at 200°C and, finally, for 6 h at 250°C. The cured product has the following ~~~~~pr _$_ properties:
291°C
Tg onset~
Tg: 301 °C
flexural strength (according to ISO 178): 144 MPa flexural elongation (according to ISO 178): 4.6 %
(T$ o~et is the point of intersection of the extended base line with the tangent at the calibzation curve in the area of the steepest ascent (measured by TMA, using a Mettler TA
3000)).
Example 2: In accordance with the general procedure described in Example 1,1 cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 20 g of a copolyether resin prepared according to Example 1 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
286°C
Tg onset~
Ts: 296°C
flexural strength (according to ISO 178): 148 MPa flexural elongation (according to ISO 178): ~.0 %
Example 3: In accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 30 g of a copolyether resin prepared according to Example 1 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
Tg onset 82 C
Tg: 292C ' flexural strength (according to ISO 178): 161 MPa flexural elongation (according to ISO 178): 5.5 %
Example 4: In accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A,10 g of a copolyether resin prepared according to Example 2 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
299°C
Tg onset~
Tg: 310°C
flexural strength (according to ISO 178): 107 MPa flexural elongation (according to ISO 178): 3.6 %
Example 5: In accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 20 g of a copolyether resin, prepared according to Example 2 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
300°C
Tg onset~
Ts: 310°C
flexural strength (according to ISO 178): 159 IvIPa flexural elongation (according to ISO 178): 5.5 %
Example 6: In accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 30 g of a copolyether resin, prepared according to Example 2 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
305°C
Tg onset Ts: 312°C
flexural strength (according to ISO 178): 157 MPa flexural elongation (according to ISO 178): 5.6 %
Example 7: In accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 10 g of a copolyether resin, prepared according to Example 5 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
Tg onset~
Ts: 312°C
flexural strength (according to - to -ISO 178): 162 MPa flexural elongation (according to ISO 178): 5.8 %
Example 8:1n accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 20 g of a copolyether resin, prepared according to Example 5 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
305°C
Tg onset Tg: 313°C
flexural strength (according to ISO 178): 165 MPa flexural elongation (according to ISO 178): 5.9 %
Example 9: In accordance with the general procedure described in Example l, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 30 g of a copolyether resin, prepared according to Example S of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
305°C
Tg onset~
Tg: 312°C
flexural strength (according to ISO 178): 167 MPa flexural elongation (according to ISO 178): 6.6 %
Example 10: In accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 50 g of a copolyether resin, prepared according to Example 5 of EP-A 327 498, and 10f? g of methylenebisphenylmaleimide. The product has the following properties:
314°C
Tg onset~
Tg: 326°C
flexural strength (according to ISO 178): 170 MPa flexural elongation (according to ISO 178): 5.7 %
Example 11: In accordance with the general procedure described in Example l, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 50 g of a copolyether resin, prepared according to Example 5 of EP-A 327 498, and 50 g of methylenebisphenylmaleimide. The product has the following properties;
°
Tg °~et: 300 C
Tg: 308°C
flexural strength (according to ISO 178): 160 MPa flexural elongation (according to ISO 178): 6.0 %
Example 12; 20 g of a copolyether resin, prepared according to Example 5 of EP-A 327 498, axe dissolved, with stirring, over 30 minutes at 150°C in 44 g of o,o'-diaIlyl bisphenol A, and a mixture of 50 g of methylenebisphenylmaleimide and 50 g of methylenebis(2-ethyl-6-methyl-phenyl)maleimide is added. The reaction mixture is stirred for a further 15 minutes at 100°C, then degassed under vacuum (10 tort) and poured into a hot aluminium mould (4 mm) of 200°C. The mixture is fully cured for 1 h at 200°C, for 2 h at 220°C and, finally, for 6 h at 280°C. The product has the following properties:
322°C
Tg onset Tg: 331°C
flexural strength (according to ISO 178): 151 MPa flexural elongation (according to ISO 178): 6.2
Preferred radicals E have the formulae XII to XIV
/ / \
). I (xrm, /. ~ ~ /
\ \ /
to wherein L is a direct bond, a group of formulae -CrH2r- (r=1 to 20) , -CH (C6H5) -, -C (CF3) 2-, -S-, -SOZ-, -O- or -CO-, or is a group of formula XV or XVI
(XV), (XV~.
Most particularly preferred radicals E have the formulae XII, XIII or XIV, wherein L is a direct bond or a group of formula -CH2-, -CH (CH3) -, -CH (C2H5) -, -C (CH3) (CZHS) -, -C (CF3) 2-, -S-, -S02- or -CO- .
Y and Z preferably have the same meaning.
Especially preferred components c) are copolyether resins comprising 2 to 30 mol % of structural repeating units of formula II and 98 to 70 mol % of structural repeating units of formula III and having an average molecular weight (number average) of 2,000 to 30,000, preferably 5,000 to 20,000.
6a The compositions of this invention preferably contain 5-100 % by weight, most preferably 10-50 % by weight of component c), based on the amount of component a).
The molar ratio of component b):a) is preferably (0.5-1.4):1, preferably (0.7-1.2):1.
The compositions of the invention are cured in known manner, typically in the temperature range from 100 to 300°C for a time sufficient to effect the cure.
The expression "cure" as used herein means the conversion of low viscosity resin compositions into insoluble and infusible crosslinked products. It is thus possible to prepare high-performance _7_ moulded articles such as (fibre-reinforced} composites, structural adhesives, laminating or electrical insulating resins which can be subjected to high temperatures.
The compositions of the invention can be mixed at any stage prior to the cure with conventional modifiers such as extenders, fillers and reinforcing agents, pigments, dyes, organic solvents, plasticisers, tackifiers, tougheners, rubbers, accelerators, flame retardants or thixotropic agents.
Illustrative examples of suitable modifiers are: coal tar, bitumen, glass fibres, boron fibres, carbon fibres, cellulose, polyethylene powder, polypropylene powder, mica, asbestos, quartz powder, gypsum, antimony trioxide, bentones, silica aerogel ("aerosil"), lithopone, barites, titanium dioxide, carbon black, graphite, iron oxide, metal powders such as aluminium powder or iron powder, silicones, cellulose acetate butyrate, polyvinyl butyrate, waxes and stearates.
Suitable additional tougheners are products which are known to the skilled parson, such as polyimicles (for example Matrimid~ 5218, Ciba-Geigy), polyether imides (for example Ultem~
1000, General Electric), polyether sulfones or ketanes (for example VlCtrex~, ICI or Ultrason~ E, BASF) or polyhydantoins.
The compositions of the invention are very readily processible, have good solubility in customary organic solvents, good stability in the melt or in solution, and the cured products made from them have good thermal and mechanical properties. The products obtained have enhanced toughness and high glass transition temperatures.
The invention accordingly also relates to a process for the preparation of cured products, which comprises the use of the novel compositions.
The compositions of this invention can be used in different fields, for example in prepregs, laminates, composites, printed circuit boards, castings, mouldings, adhesives and coatings. A
particularly interesting utility is the fabrication of fibre-reinforced composites.
Example 1 In a round flask, 75 g of o,o'-diallyl bisphenel A is heated to 150°C
and, with stirring, 10 g of a copolyether resin prepared according to Example 1 of EP-A 327 498 are added.
When the resin has completely dissolved (15 min), 100 g of methylenebisphenylmaleimide are added, with stirring.
The mixture is then stirred for a further 15 minutes at 125-130°C, degassed under a water jet vacuum, and poured into an aluminium mould (4 mm) of 180°C. The mixture is fully cured for 1 h at 180°C, for 2 h at 200°C and, finally, for 6 h at 250°C. The cured product has the following ~~~~~pr _$_ properties:
291°C
Tg onset~
Tg: 301 °C
flexural strength (according to ISO 178): 144 MPa flexural elongation (according to ISO 178): 4.6 %
(T$ o~et is the point of intersection of the extended base line with the tangent at the calibzation curve in the area of the steepest ascent (measured by TMA, using a Mettler TA
3000)).
Example 2: In accordance with the general procedure described in Example 1,1 cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 20 g of a copolyether resin prepared according to Example 1 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
286°C
Tg onset~
Ts: 296°C
flexural strength (according to ISO 178): 148 MPa flexural elongation (according to ISO 178): ~.0 %
Example 3: In accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 30 g of a copolyether resin prepared according to Example 1 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
Tg onset 82 C
Tg: 292C ' flexural strength (according to ISO 178): 161 MPa flexural elongation (according to ISO 178): 5.5 %
Example 4: In accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A,10 g of a copolyether resin prepared according to Example 2 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
299°C
Tg onset~
Tg: 310°C
flexural strength (according to ISO 178): 107 MPa flexural elongation (according to ISO 178): 3.6 %
Example 5: In accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 20 g of a copolyether resin, prepared according to Example 2 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
300°C
Tg onset~
Ts: 310°C
flexural strength (according to ISO 178): 159 IvIPa flexural elongation (according to ISO 178): 5.5 %
Example 6: In accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 30 g of a copolyether resin, prepared according to Example 2 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
305°C
Tg onset Ts: 312°C
flexural strength (according to ISO 178): 157 MPa flexural elongation (according to ISO 178): 5.6 %
Example 7: In accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 10 g of a copolyether resin, prepared according to Example 5 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
Tg onset~
Ts: 312°C
flexural strength (according to - to -ISO 178): 162 MPa flexural elongation (according to ISO 178): 5.8 %
Example 8:1n accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 20 g of a copolyether resin, prepared according to Example 5 of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
305°C
Tg onset Tg: 313°C
flexural strength (according to ISO 178): 165 MPa flexural elongation (according to ISO 178): 5.9 %
Example 9: In accordance with the general procedure described in Example l, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 30 g of a copolyether resin, prepared according to Example S of EP-A 327 498, and 100 g of methylenebisphenylmaleimide. The product has the following properties:
305°C
Tg onset~
Tg: 312°C
flexural strength (according to ISO 178): 167 MPa flexural elongation (according to ISO 178): 6.6 %
Example 10: In accordance with the general procedure described in Example 1, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 50 g of a copolyether resin, prepared according to Example 5 of EP-A 327 498, and 10f? g of methylenebisphenylmaleimide. The product has the following properties:
314°C
Tg onset~
Tg: 326°C
flexural strength (according to ISO 178): 170 MPa flexural elongation (according to ISO 178): 5.7 %
Example 11: In accordance with the general procedure described in Example l, a cured product is prepared from 75 g of o,o'-diallyl bisphenol A, 50 g of a copolyether resin, prepared according to Example 5 of EP-A 327 498, and 50 g of methylenebisphenylmaleimide. The product has the following properties;
°
Tg °~et: 300 C
Tg: 308°C
flexural strength (according to ISO 178): 160 MPa flexural elongation (according to ISO 178): 6.0 %
Example 12; 20 g of a copolyether resin, prepared according to Example 5 of EP-A 327 498, axe dissolved, with stirring, over 30 minutes at 150°C in 44 g of o,o'-diaIlyl bisphenol A, and a mixture of 50 g of methylenebisphenylmaleimide and 50 g of methylenebis(2-ethyl-6-methyl-phenyl)maleimide is added. The reaction mixture is stirred for a further 15 minutes at 100°C, then degassed under vacuum (10 tort) and poured into a hot aluminium mould (4 mm) of 200°C. The mixture is fully cured for 1 h at 200°C, for 2 h at 220°C and, finally, for 6 h at 280°C. The product has the following properties:
322°C
Tg onset Tg: 331°C
flexural strength (according to ISO 178): 151 MPa flexural elongation (according to ISO 178): 6.2
Claims (25)
1. A composition comprising a) at least one bismaleimide of formula I
wherein R1 and R2 are each independently of the other hydrogen or methyl and A is a divalent organic radical of 2 to 30 carbon atoms, b) at least one mononuclear or polynuclear alkenylphenol, an alkenylphenol ether or a mixture thereof, wherein the alkenyl group contains at least three carbon atoms, c) a copolyether resin containing end groups -OR3 attached direct to phenyl nucleic and 1 to 50 mol % of structural repeating units of formula II
and 50 to 99 mol % of structural repeating units of formula III
wherein R3 is hydrogen or a radical of formulae IV to VII
<IMGs>
X is a direct bond or a group of formulae -CrH2r-, -CH(C6H5)-, -C(CF3)2-, -S-, -SO-, -SO2-, -O- or -CO-, r is 1 to 20, R4 is prop-1-enyl or 2-methylprop-1-enyl, R5, R6 and R7 are each independently of one another C1-C4alkyl, C1-C4alkoxy or chloro or bromo, m, n and t are each independently of one another 0, 1 or
wherein R1 and R2 are each independently of the other hydrogen or methyl and A is a divalent organic radical of 2 to 30 carbon atoms, b) at least one mononuclear or polynuclear alkenylphenol, an alkenylphenol ether or a mixture thereof, wherein the alkenyl group contains at least three carbon atoms, c) a copolyether resin containing end groups -OR3 attached direct to phenyl nucleic and 1 to 50 mol % of structural repeating units of formula II
and 50 to 99 mol % of structural repeating units of formula III
wherein R3 is hydrogen or a radical of formulae IV to VII
<IMGs>
X is a direct bond or a group of formulae -CrH2r-, -CH(C6H5)-, -C(CF3)2-, -S-, -SO-, -SO2-, -O- or -CO-, r is 1 to 20, R4 is prop-1-enyl or 2-methylprop-1-enyl, R5, R6 and R7 are each independently of one another C1-C4alkyl, C1-C4alkoxy or chloro or bromo, m, n and t are each independently of one another 0, 1 or
2, p is 1 or 2. E is a divalent radical of a bisphenol after removal of both phenolic hydroxyl groups, which radical is unsubstituted or substituted by one or two C1-C4alkyl or C1-C4alkoxy groups or one or two chlorine or bromine atoms, Y
and Z are each independently of the other -CO- or -SO2-, R8 is vinyl, ethynyl, allyl, methallyl, prop-1-enyl or 2-methylprop-1-enyl, R9 and R10 are each independently of the other hydrogen, allyl or methallyl, R11 is hydrogen or methyl, q is 1 or 2, G is a group of formulae VIII or IX, wherein R12 is hydrogen or methyl and s is 0, 1 or 2.
2. A composition according to claim 1, wherein R1 and R2 are hydrogen.
and Z are each independently of the other -CO- or -SO2-, R8 is vinyl, ethynyl, allyl, methallyl, prop-1-enyl or 2-methylprop-1-enyl, R9 and R10 are each independently of the other hydrogen, allyl or methallyl, R11 is hydrogen or methyl, q is 1 or 2, G is a group of formulae VIII or IX, wherein R12 is hydrogen or methyl and s is 0, 1 or 2.
2. A composition according to claim 1, wherein R1 and R2 are hydrogen.
3. A composition according to claim 1 or 2 containing a compound of formula I, wherein A is -C2H2u-, in which a is 2-20, phenylene, xylylene, naphthylene, cyclopentylene, 1,5,5-trimethylcyclohexyl-1,3-ene; cyclohexyl-1,4-ene; 1,4-bis(methylene)cyclohexylene, the radical of 4,4'-bis(cyclohexyl)methane or a group of formula X, wherein R13 and R14 are identical or different and are each hydrogen or C1-C4alkyl, R15 and R16 are each independently of the other a hydrogen or halogen atom, and T is a direct bond, methylene, 2,2-propylidene, -S-, -SO-, -SO2-, -O- or -CO-.
4. A composition according to claim 3, wherein A is a group of formula X, wherein R13 and R14 are each independently of the other hydrogen, methyl or ethyl, R15 and R16 are hydrogen and T is methylene.
5. A composition according to claim 1, wherein the compound of formula I is methylenebis(phenylmaleimide).
6. A composition according to any one of claims 1 to 5, wherein component b) is a compound of formula XI
wherein Q is a direct bond, -CH2-, -C(CH3)2-, -S-, -SO-, -SO2-, -O- or -CO-, R17, R18, R19 and R20 are each independently of one another hydrogen or C3-C10alkenyl, and at least one of R17 to R20 is an alkenyl group, and R21 is hydrogen, C1-C10alkyl, C6-C10aryl or C3-C10alkenyl.
wherein Q is a direct bond, -CH2-, -C(CH3)2-, -S-, -SO-, -SO2-, -O- or -CO-, R17, R18, R19 and R20 are each independently of one another hydrogen or C3-C10alkenyl, and at least one of R17 to R20 is an alkenyl group, and R21 is hydrogen, C1-C10alkyl, C6-C10aryl or C3-C10alkenyl.
7. A composition according to claim 6, wherein the alkenyl group in formula XI is an allyl, methallyl or propenyl group.
8. A composition according to claim 6, wherein Q is -CH2-, -C(CH3)2-, -S-, -SO2-, -O- or -CO-, R17 and R19 are each allyl, R18 and R20 are each hydrogen and R21 is hydrogen.
9. A composition according to claim 6, wherein Q is -C(CH3)2-, R17 and R19 are each allyl, R18 and R20 are each hydrogen, and R21 is hydrogen.
10. A composition according to claim 1, wherein the indices m, n and t are 0, and p and q are 1.
11. A composition according to any one of claims 1 to 10, wherein R3 is hydrogen or a radical of formula V, wherein R9 and R10 are each hydrogen and q is 1.
12. A composition according to any one of claims 1 to 11, wherein X is a direct bond, -CH2-, -CH(CH3)-, -CH(C6H5)-, -C(CH3)2-, -C(CF3)2-, -S-, -SO-, -SO2-, -O- or -CO-.
13. A composition according to any one of claims 1 to 11, wherein X is a direct bond, -CH2- or -C(CH3)2-.
14. A composition according to any one of claims 1 to 13, wherein R4 is prop-1-enyl.
15. A composition according to any one of claims 1 to 14, wherein the substituents R4 in formula II are each in ortho-position to the phenolic -O- atom.
16. A composition according to any one of claims 1 to 15, wherein E is a group of formulae XII to XIV
wherein L is a direct bond, a group of formulae -CrH2r- (r=1 to 20) , -CH(C6H5)-, -C(CF3)2-, -S-, -SO2-, -O- or -CO-, or is a group of formula XV or XVI
wherein L is a direct bond, a group of formulae -CrH2r- (r=1 to 20) , -CH(C6H5)-, -C(CF3)2-, -S-, -SO2-, -O- or -CO-, or is a group of formula XV or XVI
17. A composition according to claim 16, wherein E is a group of formulae XII, XIII or XIV, wherein L is a direct bond or a group of formula -CH2-, -CH(CH3)-, -CH(C2H5)-, -C(CH3)(C2H5)-, -C(CF3)2-, -S-, -SO2- or -CO-.
18. A composition according to any one of claims 1 to 17, wherein Y and Z have the same meaning.
19. A composition according to any one of claims 1 to 18, wherein component c) is a copolyether resin comprising 2 to 30 mol % of structural repeating units of formula II and 98 to 70 mol % of structural repeating units of formula III and having an average molecular weight (number average) of 2,000 to 30,000.
20. A composition according to claim 19, wherein the average molecular weight (number average) is 5,000 to 20,000.
21. A composition according to any one of claims 1 to 20, which contains 5-100 % by weight of component c), based on the amount of component a).
22. A composition according to any one of claims 1 to 20, which contains 10-50% by weight of component c) based on the amount of component a).
23. A composition according to any one of claims 1 to 22, wherein the molar ratio of component b):a) is (0.5-1.4):1.
24. A composition according to claim 23, wherein the molar ratio is (0.7-1.2):1.
25. A process for the preparation of cured products, which comprises the use of a composition as claimed in any one of claims 1 to 24.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH171490 | 1990-05-21 | ||
| CH1714/90-7 | 1990-05-21 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2042857A1 CA2042857A1 (en) | 1991-11-22 |
| CA2042857C true CA2042857C (en) | 2002-09-10 |
Family
ID=4216884
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002042857A Expired - Fee Related CA2042857C (en) | 1990-05-21 | 1991-05-17 | Curable bismaleide systems |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0458744B1 (en) |
| JP (1) | JPH04227931A (en) |
| CA (1) | CA2042857C (en) |
| DE (1) | DE59105833D1 (en) |
| ES (1) | ES2074251T3 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5827907A (en) * | 1993-08-30 | 1998-10-27 | Ibm Corporation | Homo-, co- or multicomponent thermoplastic polymer dispersed in a thermoset resin |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH615935A5 (en) * | 1975-06-19 | 1980-02-29 | Ciba Geigy Ag | |
| US4288583A (en) * | 1978-12-29 | 1981-09-08 | Ciba-Geigy Corporation | Curable mixtures based on maleimides and 1-propenyl-substituted phenols |
| US4883845A (en) * | 1988-02-01 | 1989-11-28 | Ciba-Geigy Corporation | Curable composition of polyether sulfone or polyether ketone copolymer and unsaturated imide |
| US4883855A (en) * | 1988-02-01 | 1989-11-28 | Ciba-Geigy Corporation | Ethylenically unsaturated polyether sulfone or polyether ketone copolymer |
| EP0385937A1 (en) * | 1989-02-28 | 1990-09-05 | Ciba-Geigy Ag | Curable blends based on aromatic bismaleinimides |
| JPH03160036A (en) * | 1989-11-17 | 1991-07-10 | Toray Ind Inc | Thermoset resin composition for prepreg |
| JPH03162406A (en) * | 1989-11-21 | 1991-07-12 | Mitsubishi Rayon Co Ltd | Resin composition for composite material |
| EP0438378A1 (en) * | 1990-01-18 | 1991-07-24 | Ciba-Geigy Ag | Substituted diallylphenol derivatives as reactive diluents for bismaleimides |
-
1991
- 1991-05-10 DE DE59105833T patent/DE59105833D1/en not_active Expired - Fee Related
- 1991-05-10 EP EP91810363A patent/EP0458744B1/en not_active Expired - Lifetime
- 1991-05-10 ES ES91810363T patent/ES2074251T3/en not_active Expired - Lifetime
- 1991-05-17 CA CA002042857A patent/CA2042857C/en not_active Expired - Fee Related
- 1991-05-21 JP JP3145494A patent/JPH04227931A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CA2042857A1 (en) | 1991-11-22 |
| DE59105833D1 (en) | 1995-08-03 |
| EP0458744B1 (en) | 1995-06-28 |
| EP0458744A3 (en) | 1993-04-28 |
| ES2074251T3 (en) | 1995-09-01 |
| JPH04227931A (en) | 1992-08-18 |
| EP0458744A2 (en) | 1991-11-27 |
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| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKLA | Lapsed |